Clinical Safety Manager - Pharmacovigilance​/Drug Safety

Clinical Safety Manager - Pharmacovigilance / Drug Safety

Medpace Stirling, Scotland, United Kingdom

Posted 3 days ago

We are currently seeking a full‑time, office‑based Clinical Safety Manager to join our UK team at our growing office in Stirling. This position plays a key role in the pharmacovigilance process at Medpace, working in a team to accomplish tasks and projects that are instrumental to the company’s success.

This is an opportunity for an experienced professional to use expertise and develop further their career.

• Manage Clinical Safety activities and multiple large programs.
• Manage relationships with clients and internal stakeholders by providing expert safety knowledge.
• Oversee clinical safety case management and aggregate reporting responsibilities to ensure client needs are fulfilled to a high quality.
• Provide safety review of clinical study documents, including protocols, study reports, and marketing application components.
• Create safety management plans dependent upon client.
• Attend business development activities such as presentations to prospective sponsors, participation in sponsor audits, generation of scope of work and cost estimates.
• Write departmental SOPs and work instructions.

• Bachelor’s degree or equivalent and clinical safety experience, including project management and ideally line management experience.
• Previous experience of managing clinical safety activities for multiple programmes.
• Experience in writing departmental SOPs and work instructions.
• Experience in PSMF generation and maintenance.
• Experience in CCDS/RMP/SmPC writing and maintenance.
• Comprehensive knowledge of global clinical safety regulatory requirements.
• Excellent verbal and written communication skills.
• Strong leadership, mentoring, and motivational skills.
• Exceptional teamwork skills.
• Ability to work independently.

Medpace is a full‑service clinical contract research organization (CRO). We provide Phase I–IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through scientific and disciplined approaches. We leverage local regulatory and therapeutic expertise across all major therapeutic areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti‑viral and anti‑infective.

Headquartered in Cincinnati, Ohio, we employ more than 5,000 people across 40+ countries.

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company‑sponsored employee appreciation events
• Employee health and wellness initiatives

• Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024.
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.